Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion evidence source_evidence_literature NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion SIO_000772 23797140 NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion wasDerivedFrom befree-2016 NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_assertion wasGeneratedBy ECO_0000203 NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1088638.RAu01qTHc5cH1Vc3AK21lwPQZopMdPdQGZMq_lwa1VRNo130_provenance.